tetano
Editor, Senior Moderator
Sheng Wu Gong Cheng Xue Bao. 2017 Aug 25;33(8):1253-1264. doi: 10.13345/j.cjb.160483.
[h=1][Establishment of a high sensitive indirect ELISA for detecting specific antibodies against H9 subtype avian influenza virus].[/h] [Article in Chinese; Abstract available in Chinese from the publisher]
Zhang W[SUP]1,[/SUP][SUP]2[/SUP], Hou L[SUP]3[/SUP], Song J[SUP]1,[/SUP][SUP]2[/SUP], Zhang S[SUP]1[/SUP], Li Y[SUP]1[/SUP], Li J[SUP]1[/SUP], Sun L[SUP]1,[/SUP][SUP]2[/SUP], Fan W[SUP]1[/SUP], Liu W[SUP]1,[/SUP][SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] in English, Chinese
H9 subtype avian influenza virus causes worldwide epidemic, resulting in enormous economic losses of poultry production. In the present study, an indirect ELISA method was established for more accurate and specific detection. The recombinant protein of the globular head domain of HA of H9 subtype avian influenza virus was used as antigen. Specific blocking buffers and dilution buffers were determined to increase the sensitivity and specificity. The sensitivity of ELISA was higher than that of hemagglutination inhibition (HI) test. The coating antigen is very specific and no cross-reactivity with positive serum against H3N2, H5N2 and H7N9 subtype influenza viruses, Newcastle disease virus, avian infectious bronchitis virus, avian infectious disease virus, and egg drop syndrome virus. Two hundred of clinical sera samples were examined. The results indicate the coincidence rate between ELISA and HI test reached 97%. In addition, there was a positive correlation between OD450 values and the logarithm of HI titer to the base 2 of an individual serum sample (R2=0.981 1).
[h=4]KEYWORDS:[/h] H9 subtype; avian influenza virus; hemagglutination inhibition test; hemagglutinin; indirect ELISA
PMID: 28853253 DOI: 10.13345/j.cjb.160483
[h=1][Establishment of a high sensitive indirect ELISA for detecting specific antibodies against H9 subtype avian influenza virus].[/h] [Article in Chinese; Abstract available in Chinese from the publisher]
Zhang W[SUP]1,[/SUP][SUP]2[/SUP], Hou L[SUP]3[/SUP], Song J[SUP]1,[/SUP][SUP]2[/SUP], Zhang S[SUP]1[/SUP], Li Y[SUP]1[/SUP], Li J[SUP]1[/SUP], Sun L[SUP]1,[/SUP][SUP]2[/SUP], Fan W[SUP]1[/SUP], Liu W[SUP]1,[/SUP][SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] in English, Chinese
H9 subtype avian influenza virus causes worldwide epidemic, resulting in enormous economic losses of poultry production. In the present study, an indirect ELISA method was established for more accurate and specific detection. The recombinant protein of the globular head domain of HA of H9 subtype avian influenza virus was used as antigen. Specific blocking buffers and dilution buffers were determined to increase the sensitivity and specificity. The sensitivity of ELISA was higher than that of hemagglutination inhibition (HI) test. The coating antigen is very specific and no cross-reactivity with positive serum against H3N2, H5N2 and H7N9 subtype influenza viruses, Newcastle disease virus, avian infectious bronchitis virus, avian infectious disease virus, and egg drop syndrome virus. Two hundred of clinical sera samples were examined. The results indicate the coincidence rate between ELISA and HI test reached 97%. In addition, there was a positive correlation between OD450 values and the logarithm of HI titer to the base 2 of an individual serum sample (R2=0.981 1).
[h=4]KEYWORDS:[/h] H9 subtype; avian influenza virus; hemagglutination inhibition test; hemagglutinin; indirect ELISA
PMID: 28853253 DOI: 10.13345/j.cjb.160483